ZMP
ENSDARG00000086831
Ensembl ID:
Human Orthologues:
ZFP62, ZNF268, ZNF585A, ZNF585B, ZNF624
Human Descriptions:
zinc finger protein 268 [Source:HGNC Symbol;Acc:13061]
zinc finger protein 585A [Source:HGNC Symbol;Acc:26305]
zinc finger protein 585B [Source:HGNC Symbol;Acc:30948]
zinc finger protein 62 homolog (mouse) [Source:HGNC Symbol;Acc:23241]
zinc finger protein 624 [Source:HGNC Symbol;Acc:29254]
zinc finger protein 585A [Source:HGNC Symbol;Acc:26305]
zinc finger protein 585B [Source:HGNC Symbol;Acc:30948]
zinc finger protein 62 homolog (mouse) [Source:HGNC Symbol;Acc:23241]
zinc finger protein 624 [Source:HGNC Symbol;Acc:29254]
Mouse Orthologues:
5430403G16Rik, Gm13212, Gm14124, Gm14295, Zfp26, Zfp27, Zfp619, Zfp62, Zfp658, Zfp788, Zfp808, Zfp873
Mouse Descriptions:
RIKEN cDNA 5430403G16 gene Gene [Source:MGI Symbol;Acc:MGI:1924450]
predicted gene 13212 Gene [Source:MGI Symbol;Acc:MGI:3651014]
predicted gene 14124 Gene [Source:MGI Symbol;Acc:MGI:3652002]
predicted gene 14295 Gene [Source:MGI Symbol;Acc:MGI:3709624]
zinc finger protein 26 Gene [Source:MGI Symbol;Acc:MGI:99173]
zinc finger protein 27 Gene [Source:MGI Symbol;Acc:MGI:99174]
zinc finger protein 619 Gene [Source:MGI Symbol;Acc:MGI:1917477]
zinc finger protein 62 Gene [Source:MGI Symbol;Acc:MGI:99662]
zinc finger protein 658 Gene [Source:MGI Symbol;Acc:MGI:2652821]
zinc finger protein 788 Gene [Source:MGI Symbol;Acc:MGI:1914857]
zinc finger protein 80 Gene [Source:MGI Symbol;Acc:MGI:3704127]
zinc finger protein 873 Gene [Source:MGI Symbol;Acc:MGI:3040689]
predicted gene 13212 Gene [Source:MGI Symbol;Acc:MGI:3651014]
predicted gene 14124 Gene [Source:MGI Symbol;Acc:MGI:3652002]
predicted gene 14295 Gene [Source:MGI Symbol;Acc:MGI:3709624]
zinc finger protein 26 Gene [Source:MGI Symbol;Acc:MGI:99173]
zinc finger protein 27 Gene [Source:MGI Symbol;Acc:MGI:99174]
zinc finger protein 619 Gene [Source:MGI Symbol;Acc:MGI:1917477]
zinc finger protein 62 Gene [Source:MGI Symbol;Acc:MGI:99662]
zinc finger protein 658 Gene [Source:MGI Symbol;Acc:MGI:2652821]
zinc finger protein 788 Gene [Source:MGI Symbol;Acc:MGI:1914857]
zinc finger protein 80 Gene [Source:MGI Symbol;Acc:MGI:3704127]
zinc finger protein 873 Gene [Source:MGI Symbol;Acc:MGI:3040689]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19946 | Nonsense | Available for shipment | Available now |
| sa39986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39987 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25991 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33089 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19946
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127809 | Nonsense | 226 | 862 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 7582671)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 7121815 |
| GRCz11 | 3 | 7007655 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACCATTCAGATGCACTCAGTGTGGGAAGAGTTTCGGTCGATCATCA[C/T]AGCATGATATACACATGAAGAGCCACACTGGTGTGAGAGAGTATGTTTGC
Long Flanking Sequence:
TCAATCTACACATGATGATCCACACTGGAGAGAAACCATTCACGTGCACTCAGTGTGGCAAGAGCTTCATCCAATCATCGTCCCTTAATCTACATATGAGAATCCACACTGGAGAGAAACCATTCAGATGCACTCAGTGTGGGAAGAGTTTCAGCCAATCATCATCCCTTAATCTACACATGAGGATTCACACTGGAAAGAAACCATTCACATGTACTCAGTGTGGGAAGAGCTTCAACCAATCATCAAACCTTAATCAACACATGAAGATTCACACTGGAGAAAAACCATTCACGTGCATTCAGTGTGGAAAGAGTTTCAGCCAATCATCAAACCTTAATCACCACATGAGGATCCACACTGGAGAGAAACCATTCACATGTACTCGGTGTGGGAAGGGTTTCAGCCAGTCATCATCCCTTAATCTACACATGAGGATCCACACTGGAGAGAAACCATTCAGATGCACTCAGTGTGGGAAGAGTTTCGGTCGATCATCA[C/T]AGCATGATATACACATGAAGAGCCACACTGGTGTGAGAGAGTATGTTTGCTTTGAGTGTGAGAAAACCTTTATTACATCTGGAGAGTTGAAACTGCACCAGAGGAATCACGCTGGGGAGAAACCGTACAAGTGTTCACACTGCGACAAGAGGTTTAATCAGTCAGAACATCTGAAAAGACATGAGAGGACTCACACTGGAGAGAAACCGTACATGTGTTCACACTGCAACAAGAGATTCAGTCAGTTACCACATTTGAAAACACATGAGAGGATTCACACTGGAGAGAAACCGTACAGATGTGATCAGTGTCTACAGAGTTTCGCTCATTTGGTGCAGCTTAAGAAACACATGGACCAAAAGCTGCACACATGACATGAATACAGCATAACATTTTTTTTTATATGCAAAGGAGCTTTTGGTTTGGTGTGCACCCCCCTTTGAGTCCTTAAAATCTCTCTGCGAGTGATCCTACAGATGCGGATACATCTGTACAGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39986
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127809 | Nonsense | 259 | 862 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 7582770)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 7121914 |
| GRCz11 | 3 | 7007754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTGAGTGTGAGAAAACCTTTATTACATCTGGAGAGTTGAAACTGCAC[C/T]AGAGGAATCACGCTGGGGAGAAACCGTACAAGTGTTCACACTGCGACAAG
Long Flanking Sequence:
GAATCCACACTGGAGAGAAACCATTCAGATGCACTCAGTGTGGGAAGAGTTTCAGCCAATCATCATCCCTTAATCTACACATGAGGATTCACACTGGAAAGAAACCATTCACATGTACTCAGTGTGGGAAGAGCTTCAACCAATCATCAAACCTTAATCAACACATGAAGATTCACACTGGAGAAAAACCATTCACGTGCATTCAGTGTGGAAAGAGTTTCAGCCAATCATCAAACCTTAATCACCACATGAGGATCCACACTGGAGAGAAACCATTCACATGTACTCGGTGTGGGAAGGGTTTCAGCCAGTCATCATCCCTTAATCTACACATGAGGATCCACACTGGAGAGAAACCATTCAGATGCACTCAGTGTGGGAAGAGTTTCGGTCGATCATCACAGCATGATATACACATGAAGAGCCACACTGGTGTGAGAGAGTATGTTTGCTTTGAGTGTGAGAAAACCTTTATTACATCTGGAGAGTTGAAACTGCAC[C/T]AGAGGAATCACGCTGGGGAGAAACCGTACAAGTGTTCACACTGCGACAAGAGGTTTAATCAGTCAGAACATCTGAAAAGACATGAGAGGACTCACACTGGAGAGAAACCGTACATGTGTTCACACTGCAACAAGAGATTCAGTCAGTTACCACATTTGAAAACACATGAGAGGATTCACACTGGAGAGAAACCGTACAGATGTGATCAGTGTCTACAGAGTTTCGCTCATTTGGTGCAGCTTAAGAAACACATGGACCAAAAGCTGCACACATGACATGAATACAGCATAACATTTTTTTTTATATGCAAAGGAGCTTTTGGTTTGGTGTGCACCCCCCTTTGAGTCCTTAAAATCTCTCTGCGAGTGATCCTACAGATGCGGATACATCTGTACAGCTCTGCTGCTTCACTGTCCAGTGTGTTCATGTGGCTAGTGTTGTTGTTTTGGATGATGTTCTCTGTCTGACCCACTCAATGAGAAACAACTCAATGGGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39987
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127809 | Nonsense | 311 | 862 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 7582927)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 7122071 |
| GRCz11 | 3 | 7007911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGTACATGTGTTCACACTGCAACAAGAGATTCAGTCAGTTACCACATT[T/A]GAAAACACATGAGAGGATTCACACTGGAGAGAAACCGTACAGATGTGATC
Long Flanking Sequence:
TCAACACATGAAGATTCACACTGGAGAAAAACCATTCACGTGCATTCAGTGTGGAAAGAGTTTCAGCCAATCATCAAACCTTAATCACCACATGAGGATCCACACTGGAGAGAAACCATTCACATGTACTCGGTGTGGGAAGGGTTTCAGCCAGTCATCATCCCTTAATCTACACATGAGGATCCACACTGGAGAGAAACCATTCAGATGCACTCAGTGTGGGAAGAGTTTCGGTCGATCATCACAGCATGATATACACATGAAGAGCCACACTGGTGTGAGAGAGTATGTTTGCTTTGAGTGTGAGAAAACCTTTATTACATCTGGAGAGTTGAAACTGCACCAGAGGAATCACGCTGGGGAGAAACCGTACAAGTGTTCACACTGCGACAAGAGGTTTAATCAGTCAGAACATCTGAAAAGACATGAGAGGACTCACACTGGAGAGAAACCGTACATGTGTTCACACTGCAACAAGAGATTCAGTCAGTTACCACATT[T/A]GAAAACACATGAGAGGATTCACACTGGAGAGAAACCGTACAGATGTGATCAGTGTCTACAGAGTTTCGCTCATTTGGTGCAGCTTAAGAAACACATGGACCAAAAGCTGCACACATGACATGAATACAGCATAACATTTTTTTTTATATGCAAAGGAGCTTTTGGTTTGGTGTGCACCCCCCTTTGAGTCCTTAAAATCTCTCTGCGAGTGATCCTACAGATGCGGATACATCTGTACAGCTCTGCTGCTTCACTGTCCAGTGTGTTCATGTGGCTAGTGTTGTTGTTTTGGATGATGTTCTCTGTCTGACCCACTCAATGAGAAACAACTCAATGGGAAGAAACCATACATCAAAGAATGCAGAGCTCCAGGACACGCCCGTATCCACACTGGAAGAGAGATCATCATCTACAGCTTAACCTCGCGAAAACGGAAATGCTTTCTGCCAACCCGACTCTACACCAAAACTTTTCAATCCAGATGGACGGGGCAACCATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25991
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127809 | Nonsense | 520 | 862 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 7602402)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 7141546 |
| GRCz11 | 3 | 7027386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGAAACCAGAAAATACATGAGAGGATTCACACTGGAGAGAGACCGTA[T/G]AAGTGTTCACACTGCGGCATGAGATTCGGTCAGTTATCAAATCTGAAATC
Long Flanking Sequence:
ACATGTTCTCAGTGCGGGAAGAGTTTTAGAGACTCATCAAACCTTAATAGACACATGTTGATCCACTCTGGAGAGAAAACACACTCATGTGATCAATGCGGAAAATCATTTCTGTTGGCTTCAAAGCTGAATGATCACCTTAGAGTTCATGCAACTGAGAAGCCTTCATGCTCTGTGTGTGGAAAGAGTTTTGCACATGAAGTAAATTTAAGAAGACATCAGAAGATCCACACCGGTGTGAGAGAGTATGTGTGCTCTGAGTGTGGGAAGACTTTTTTTACATCTACAAGCTTACAACAACACCAGATGATTCACACTGGAGAGAAACCGTACAAGTGTTCACACTGCGACAAGAGATTCAGTCAGTTAAGAAACCAGAAAATACATGAGATGATTCACACTGAAGAGAAACTGTACAAGTGTTCACACTGCGACAAAAGATTCAATTGGTTAGGAAACCAGAAAATACATGAGAGGATTCACACTGGAGAGAGACCGTA[T/G]AAGTGTTCACACTGCGGCATGAGATTCGGTCAGTTATCAAATCTGAAATCACATGAGAGGATTCACACTGGAGAGAAACCGTACAAGTGTTCACACTGCAACAAGAGATTCAGTCAGTTTAGAAGCCTGAAATCACATGTGAGGATTCACACTGGAGATACAGATATGCAAACTTGCAGTATTGATGGGTCGTTCTGGAACAAATCTTTAATGTGACTCTGCAATAATGAGTCCTTTCAGAGTGATTCCTTCATTGCTGTATGTGCAGAAAGGGGAAATGATTGATTATTTTATATTCTATCAGGTTTGAGTCGTTCATTATTCACATGAAATATCTGTAGATCCATCCTCTATGCACTTTGAGCTGCAAAAAAAATTAGTCATATTTTCAAGTCCTCTGGTTTTGGAGTTGTTTGTCTTTACATGTAACTTGACAGCAGAAAATCATTTGAATTTATACGAATTAGCCACTATATCAAAAAGTTACGAATTGCCGTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33089
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000127809 | Nonsense | 733 | 862 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 7616145)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 7155289 |
| GRCz11 | 3 | 7041129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAAACCATACAAGTGTTCACACTGCGACAAAAGATTCGGTCGGTTAT[C/A]AAATATGAAAATACATGAGAGGATTCACACTGGAGAGAAACCTTATACCT
Long Flanking Sequence:
TCTCAAGATCCACATGCGGATCCACACTGGAGAGAGACCATTCACATGTTCTCAGTGTGGGATGAGTTTCAAAGACTCATCAGCCCTTAGAAGACACATGTTGATCCACACTGGAAAGAAAGCACACACATGTGATCAGTGCGGAAAATCATTTAGGTTGTCTTCAGGCCTGAATGATCACCTTAGAGTTCATGCAACTGAGAAGCCATATTCATGCACTGTGTGTGGAAAGAGTTTTGCACATCAAGTAAATTTAAGAAGACATCAGAAGATCCACAACAGTGTGAGAGAGTATGTGTGCTCTGAGTGTGAGAAGACCTTTGTTACAGCTGCAAACTTACAACAACACCAGATGATTCACAGTGGAGAAAAACGATACAAGTGTTCACACTGCGACATGAGATTCAGTTGGTTAGGATGCCAGAAAACACATGAGAGGACTCACACCGGAGAGAAACCATACAAGTGTTCACACTGCGACAAAAGATTCGGTCGGTTAT[C/A]AAATATGAAAATACATGAGAGGATTCACACTGGAGAGAAACCTTATACCTGTTCACACTGCGACAAAAGATTCAGTCAGTTAAGAAACCTGATAACACATGAGAGGATTCACACTGGAGAAAAACCTTATCCGTGTTCACACTGCGACAAGAGATTCAGTCAGTTAGTAAGCCAGAAATCACATGAGAGGACTCACACTGGAGAGAAACCGTACAGCTGTTCACACTGCGACAAGAAATTCAGTAAGTTAAGAAGCCTGAAATCACATGAGAGGATTCACACTGAAGAGAGACCGTACAGCTGTTCACACTGCGACAAGAAATTCAGTAAGTTAAGAAGCCTGAAAACACATGAGAGGACTCACACTGGACAGAAACAAGTGAGATTCAGTCAGTCAGAAACATTGAAAAACACACAAGAGTGTCACGTCTGAGAGTAACCTTAACAGATATGCAAACTTGCAGTATTGATGGGTTGTTCTGGAACAAATCTTTAATGTG
Associated Phenotype:
Not determined